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Diclofenac Sodium

NDC 80425-0102, Diclofenac Sodium, tablet, delayed release, from Advanced Rx of Tennessee, LLC.

Product NDC
80425-0102
Status
Listed
Labeler
Advanced Rx of Tennessee, LLC
Dosage form
TABLET, DELAYED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA090066
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/80425-0102 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • DICLOFENAC SODIUM50 mg/1

Pharmacologic classes

Anti-Inflammatory Agents, Non-Steroidal [CS]; Cyclooxygenase Inhibitors [MoA]; Decreased Prostaglandin Production [PE]; Nonsteroidal Anti-inflammatory Drug [EPC]

Package NDCNDC-11Package
80425-0102-28042501020260 TABLET, DELAYED RELEASE in 1 BOTTLE (80425-0102-2)
80425-0102-38042501020390 TABLET, DELAYED RELEASE in 1 BOTTLE (80425-0102-3)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/b3dbd981-453c-645f-e053-2a95a90aec3c

Use it

Look up 80425-0102 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/80425-0102 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 80425-0102. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
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Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.